NDC 13811-629
BENAZEPRIL HYDROCHLORIDE
Benazepril Hydrochloride
BENAZEPRIL HYDROCHLORIDE is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Trigen Laboratories, Inc.. The primary component is Benazepril Hydrochloride.
| Product ID | 13811-629_df70c619-a81f-48c3-8ec7-0135dc1fb450 |
| NDC | 13811-629 |
| Product Type | Human Prescription Drug |
| Proprietary Name | BENAZEPRIL HYDROCHLORIDE |
| Generic Name | Benazepril Hydrochloride |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2012-11-15 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076118 |
| Labeler Name | Trigen Laboratories, Inc. |
| Substance Name | BENAZEPRIL HYDROCHLORIDE |
| Active Ingredient Strength | 20 mg/1 |
| Pharm Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |